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  • 2020-2024  (14)
  • 1995-1999  (186)
  • 1955-1959  (6)
  • 1940-1944  (12)
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  • 1
    Keywords: Biotechnology. ; Biomedical engineering. ; Biotechnology. ; Biomedical Engineering and Bioengineering.
    Description / Table of Contents: 1.Confocal laser scanning microscopy and fluorescence correlation methods for evaluation of molecular interactions -- 2.Number and Brightness Imaging: visualization of protein oligomerization state in living cell -- 3.Single-molecule analysis on the coupling of molecular state and reaction kinetics -- 4.Imaging lipid rafts in the plasma membrane using novel probe and super-resolution microscopy -- 5.Multiplex Immunohistochemistry (IHC) -- 6.Micro-endoscopy for live small animal fluorescent imaging -- 7.Immuno-gold techniques -- 8.Correlative Light and Electron Microscopy for Nanoparticle-Cell Interaction -- 9.Diagnostic and Therapeutic Nanomedicine -- 10.Semiconductor nanocrystals for biological imaging and fluorescence spectroscopy -- 11.DNA/RNA fluorescence imaging by synthetic nucleic acids -- Section II: Label-free techniques and advanced tomographic imaging -- 12.“Magnetic resonance imaging for preclinical study -- 13.Holotomography techniques for 3D label-free imaging of live cells and tissues -- 14.Dynamic-contrast optical imaging techniques -- 15.Emerging biological and clinical applications of photoacoustic tomography -- Section III: Potential (synergic) biotechnologies to be joined with imaging techniques -- 16.Generation of genetically-engineered mouse models using CRISPR-Cas system -- 17.Highly efficient generation of cell lines stably expressing genes of interest via Cre recombinase mediated knock-in method in mouse embryonic stem (ES) cells and its application for microscopic imaging techniques -- 18.Mass spectrometry based metabolomics in translational research -- 19.Application of mass spectrometry in drug metabolism and pharmacokinetics for drug development -- 20.Discovery and Application of Chemical Probes for Translational Research -- 21.Regeneration of skin cells by mesenchymal stem cell-derived exosomes.
    Abstract: This book is a wide-ranging guide to advanced imaging techniques and related methods with important applications in translational research or convergence science as progress is made toward a new era in integrative healthcare. Conventional and advanced microscopic imaging techniques, including both non-fluorescent (i.e., label-free) and fluorescent methods, have to date provided researchers with specific and quantitative information about molecules, cells, and tissues. Now, however, the different imaging techniques can be correlated with each other and multimodal methods developed to simultaneously obtain diverse and complementary information. In addition, the latest advanced imaging techniques can be integrated with non-imaging techniques such as mass spectroscopic methods, genome editing, organic/inorganic probe synthesis, nanomedicine, and drug discovery. The book will be of high value for researchers in the biological and biomedical sciences or convergence science who need to use these multidisciplinary and integrated techniques or are involved in developing new analytical methods focused on convergence science. .
    Type of Medium: Online Resource
    Pages: VI, 564 p. 191 illus., 161 illus. in color. , online resource.
    Edition: 1st ed. 2021.
    ISBN: 9789813360648
    Series Statement: Advances in Experimental Medicine and Biology, 1310
    DDC: 660.6
    Language: English
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  • 2
    Keywords: Sustainability. ; Digital humanities. ; Internet of things. ; Sociology, Urban. ; Urban economics. ; Architecture. ; Sustainability. ; Digital Humanities. ; Internet of Things. ; Urban Sociology. ; Urban Economics. ; Cities, Countries, Regions.
    Description / Table of Contents: Introduction - The digital polis and its practices: Beyond gated communities -- Digital polis and the ‘safe’ feminism: Focusing on the strategies of direct punishment and gated community -- Toward digital polis: Gendered data (in)justice and data activism in South Korea -- Subjection or subjectification: representation of 'networked individuals' in Korean web novels -- Digital polis and urban commons: Justice beyond the gated community -- Production and reproduction of space and culture in the virtual realm: Gated communities as the imaginary, intermediary and real spaces -- The ghettoised city and the affect of anxiety in Park Wan-soe’s ‘apartment novels’ -- Spatial and digital fortressing of apartment complexes in Seoul: Two case studies -- Inclusion, exclusion, and participation in digital polis: Double-edged development of poor urban communities in alternative smart city-making -- Online-based food hubs for community health and well-being: Performance in practice and its implications for urban design -- Third places: The social infrastructure of the smart city. .
    Abstract: This edited collection provides an alternative discourse on cities evolving with physically and virtually networked communities—the ‘digital polis’—and offers a variety of perspectives from the humanities, media studies, geography, architecture, and urban studies. As an emergent concept that encompasses research and practice, the digital polis is oriented toward a counter-mapping of the digital cityscape beyond policing and gatekeeping in physical and virtual gated communities. Considering the digital polis as offering potential for active support of socially just and politically inclusive urban circumstances in ways that mirror the Greek polis, our attention is drawn towards the interweaving of the development of digital technology, urban space, and social dynamics. The four parts of this book address the formation of technosocial subjectivity, real-and-virtual combined urbanity, the spatial dimensions of digital exclusion and inclusion, and the prospect of emancipatory and empowering digital citizens. Individual chapters cover varied topics on digital feminism, data activism, networked individualism, digital commons, real-virtual communalism, the post-family imagination, digital fortress cities, rights to the smart city, online foodscapes, and open-source urbanism across the globe. Contributors explore the following questions: what developments can be found over recent decades in both physical and virtual communities such as cyberspace, and what will our urban future be like? What is the ‘digital polis’ and what kinds of new subjectivity does it produce? How does digital technology, as well as its virtuality, reshape the city and our spatial awareness of it? What kinds of exclusion and cooperation are at work in communities and spaces in the digital age? Each chapter responds to these questions in its own way, navigating readers through routes toward the digital polis. Chapter "Introduction - The digital polis and its practices: Beyond gated communities" is available open access under a Creative Commons Attribution 4.0 International License via link.springer.com.
    Type of Medium: Online Resource
    Pages: VIII, 208 p. 32 illus., 27 illus. in color. , online resource.
    Edition: 1st ed. 2023.
    ISBN: 9789811996856
    Series Statement: Advances in 21st Century Human Settlements,
    DDC: 304.2
    Language: English
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  • 3
    Publication Date: 2024-03-15
    Description: Ocean warming is altering the biogeographical distribution of marine organisms. In the tropics, rising sea surface temperatures are restructuring coral reef communities with sensitive species being lost. At the biogeographical divide between temperate and tropical communities, warming is causing macroalgal forest loss and the spread of tropical corals, fishes and other species, termed “tropicalization”. A lack of field research into the combined effects of warming and ocean acidification means there is a gap in our ability to understand and plan for changes in coastal ecosystems. Here, we focus on the tropicalization trajectory of temperate marine ecosystems becoming coral-dominated systems. We conducted field surveys and in situ transplants at natural analogues for present and future conditions under (i) ocean warming and (ii) both ocean warming and acidification at a transition zone between kelp and coral-dominated ecosystems. We show that increased herbivory by warm-water fishes exacerbates kelp forest loss and that ocean acidification negates any benefits of warming for range extending tropical corals growth and physiology at temperate latitudes. Our data show that, as the combined effects of ocean acidification and warming ratchet up, marine coastal ecosystems lose kelp forests but do not gain scleractinian corals. Ocean acidification plus warming leads to overall habitat loss and a shift to simple turf-dominated ecosystems, rather than the complex coral-dominated tropicalized systems often seen with warming alone. Simplification of marine habitats by increased CO2 levels cascades through the ecosystem and could have severe consequences for the provision of goods and services.
    Keywords: Acropora solitaryensis; Alkalinity, total; Alkalinity, total, standard deviation; Animalia; Aragonite saturation state; Aragonite saturation state, standard deviation; Area/locality; Benthic animals; Benthos; Bicarbonate ion; Bottles or small containers/Aquaria (〈20 L); Calcification/Dissolution; Calcification rate of calcium carbonate; Calcite saturation state; Calculated using seacarb after Nisumaa et al. (2010); Carbon, inorganic, dissolved; Carbon, inorganic, dissolved, standard deviation; Carbonate ion; Carbonate system computation flag; Carbon dioxide; Cnidaria; CO2 vent; Coast and continental shelf; Color description; Community composition and diversity; Coral; Diameter; Entire community; Event label; EXP; Experiment; Field experiment; Field observation; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Growth/Morphology; Growth rate; Identification; Izu_Peninsula; Laboratory experiment; Month; Net calcification rate of calcium carbonate, dark; Net calcification rate of calcium carbonate, light; Net photosynthesis rate, oxygen; North Pacific; OA-ICC; Ocean Acidification International Coordination Centre; Partial pressure of carbon dioxide, standard deviation; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); pH; pH, standard deviation; Photosynthetic efficiency; Porites heronensis; Primary production/Photosynthesis; Registration number of species; Respiration; Respiration rate, oxygen; Rocky-shore community; Salinity; Shikine_Island_OAW; Shikine_Island_OW; Shoots; Single species; Site; Species; Species, unique identification; Species, unique identification (URI); Temperate; Temperature; Temperature, water; Temperature, water, standard deviation; Treatment; Type
    Type: Dataset
    Format: text/tab-separated-values, 33452 data points
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  • 4
    Publication Date: 2024-03-15
    Description: The effects of ocean acidification on ecosystems remain poorly understood, because it is difficult to simulate the effects of elevated CO2 on entire marine communities. Natural systems enriched in CO2 are being used to help understand the long-term effects of ocean acidification in situ. Here, we compared biofilm bacterial communities on intertidal cobbles/boulders and bedrock along a seawater CO2 gradient off Japan. Samples sequenced for 16S rRNA showed differences in bacterial communities with different pCO2 and between habitat types. In both habitats, bacterial diversity increased in the acidified conditions. Differences in pCO2 were associated with differences in the relative abundance of the dominant phyla. However, despite the differences in community composition, there was no indication that these changes would be significant for nutrient cycling and ecosystem function. As well as direct effects of seawater chemistry on the biofilm, increased microalgal growth and decreased grazing may contribute to the shift in bacterial composition at high CO2, as documented by other studies. Thus, the effects of changes in bacterial community composition due to globally increasing pCO2 levels require further investigation to assess the implications for marine ecosystem function. However, the apparent lack of functional shifts in biofilms along the pCO2 gradient is a reassuring indicator of stability of their ecosystem functions in shallow ocean margins.
    Keywords: ACE richness; Alkalinity, total; Aragonite saturation state; Benthos; Bicarbonate ion; Calcite saturation state; Calculated using seacarb after Nisumaa et al. (2010); Carbon, inorganic, dissolved; Carbonate ion; Carbonate system computation flag; Carbon dioxide; Chao 1 richness; CO2 vent; Coast and continental shelf; Community composition and diversity; Entire community; EXP; Experiment; Field observation; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Group; LATITUDE; LONGITUDE; North Pacific; OA-ICC; Ocean Acidification International Coordination Centre; Oxygen, dissolved; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); pH; Potentiometric; Potentiometric titration; Rocky-shore community; Salinity; Shannon Diversity Index; Shikine_Island; Simpson index of diversity; Site; Species richness; Temperate; Temperature, water; Type
    Type: Dataset
    Format: text/tab-separated-values, 864 data points
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  • 5
    Publication Date: 2024-03-15
    Description: Human activities are rapidly changing the structure and function of coastal marine ecosystems. Large-scale replacement of kelp forests and coral reefs with turf algal mats is resulting in homogenous habitats that have less ecological and human value. Ocean acidification has strong potential to substantially favour turf algae growth, which led us to examine the mechanisms that stabilise turf algal states. Here we show that ocean acidification promotes turf algae over corals and macroalgae, mediating new habitat conditions that create stabilising feedback loops (altered physicochemical environment and microbial community, and an inhibition of recruitment) capable of locking turf systems in place. Such feedbacks help explain why degraded coastal habitats persist after being initially pushed past the tipping point by global and local anthropogenic stressors. An understanding of the mechanisms that stabilise degraded coastal habitats can be incorporated into adaptive management to better protect the contribution of coastal systems to human wellbeing.
    Keywords: Alkalinity, total; Alkalinity, total, standard deviation; Aragonite saturation state; Aragonite saturation state, standard deviation; Benthos; Bicarbonate ion; Bicarbonate ion, standard deviation; Calcite saturation state; Calcite saturation state, standard deviation; Calculated using CO2SYS; Calculated using seacarb after Nisumaa et al. (2010); Calculated using seacarb after Orr et al. (2018); Carbon, inorganic, dissolved; Carbon, inorganic, dissolved, standard deviation; Carbonate ion; Carbonate ion, standard deviation; Carbonate system computation flag; Carbon dioxide; Carbon dioxide, standard deviation; CO2 vent; Coast and continental shelf; Community composition and diversity; Coverage; Distance; Entire community; EXP; Experiment; Field experiment; Figure; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Fugacity of carbon dioxide in seawater, standard deviation; North Pacific; OA-ICC; Ocean Acidification International Coordination Centre; Partial pressure of carbon dioxide, standard deviation; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); pH; pH, standard deviation; Potentiometric titration; Recruitment; Replicate; Rocky-shore community; Salinity; Salinity, standard deviation; Shikine; Site; Temperate; Temperature, water; Temperature, water, standard deviation; Transect number; Treatment; Type
    Type: Dataset
    Format: text/tab-separated-values, 5866 data points
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  • 6
    Publication Date: 2024-03-15
    Description: Diatoms are so important in ocean food-webs that any human induced changes in their abundance could have major effects on the ecology of our seas. The large chain-forming diatom Biddulphia biddulphiana greatly increases in abundance as pCO2 increases along natural seawater CO2 gradients in the north Pacific Ocean. In areas with reference levels of pCO2, it was hard to find, but as seawater carbon dioxide levels rose, it replaced seaweeds and became the main habitat-forming species on the seabed. This diatom algal turf supported a marine invertebrate community that was much less diverse and completely differed from the benthic communities found at present-day levels of pCO2. Seawater CO2 enrichment stimulated the growth and photosynthetic efficiency of benthic diatoms, but reduced the abundance of calcified grazers such as gastropods and sea urchins. These observations suggest that ocean acidification will shift photic zone community composition so that coastal food-web structure and ecosystem function are homogenised, simplified, and more strongly affected by seasonal algal blooms.
    Keywords: Alkalinity, total; Alkalinity, total, standard deviation; Aragonite saturation state; Aragonite saturation state, standard deviation; Bicarbonate ion; Bicarbonate ion, standard deviation; Calcite saturation state; Calcite saturation state, standard deviation; Calculated using CO2SYS; Calculated using seacarb after Nisumaa et al. (2010); Calculated using seacarb after Orr et al. (2018); Carbon, inorganic, dissolved; Carbon, inorganic, dissolved, standard deviation; Carbonate ion; Carbonate ion, standard deviation; Carbonate system computation flag; Carbon dioxide; Carbon dioxide, standard deviation; Diatoms; EXP; Experiment; Fluorescence, maximum; Fluorescence, minimum; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Fugacity of carbon dioxide in seawater, standard deviation; Gross primary production of oxygen per chlorophyll a; Light saturation point; Maximal absolute electron transfer rate; Maximum light use efficiency; Maximum photochemical quantum yield of photosystem II; Net primary production of oxygen per chlorophyll a; Number; Partial pressure of carbon dioxide, standard deviation; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); pH; pH, standard deviation; Potentiometric; Potentiometric titration; Registration number of species; Replicates; Respiration rate oxygen per chlorophyll a; Salinity; Salinity, standard deviation; Shikine; Site; Species; Species richness; Temperature, water; Temperature, water, standard deviation; Type; Uniform resource locator/link to reference
    Type: Dataset
    Format: text/tab-separated-values, 17717 data points
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  • 7
    Publication Date: 2024-03-15
    Description: Long‐term exposure to CO2‐enriched waters can considerably alter marine biological community development, often resulting in simplified systems dominated by turf algae that possess reduced biodiversity and low ecological complexity. Current understanding of the underlying processes by which ocean acidification alters biological community development and stability remains limited, making the management of such shifts problematic. Here, we deployed recruitment tiles in reference (pHT 8.137 +/- 0.056 SD) and CO2‐enriched conditions (pHT 7.788 +/- 0.105 SD) at a volcanic CO2 seep in Japan to assess the underlying processes and patterns of algal community development. We assessed (i) algal community succession in two different seasons (Cooler months: January–July, and warmer months: July–January), (ii) the effects of initial community composition on subsequent community succession (by reciprocally transplanting preestablished communities for a further 6 months), and (iii) the community production of resulting communities, to assess how their functioning was altered (following 12 months recruitment). Settlement tiles became dominated by turf algae under CO2‐enrichment and had lower biomass, diversity and complexity, a pattern consistent across seasons. This locked the community in a species‐poor early successional stage. In terms of community functioning, the elevated pCO2 community had greater net community production, but this did not result in increased algal community cover, biomass, biodiversity or structural complexity. Taken together, this shows that both new and established communities become simplified by rising CO2 levels. Our transplant of preestablished communities from enriched CO2 to reference conditions demonstrated their high resilience, since they became indistinguishable from communities maintained entirely in reference conditions. This shows that meaningful reductions in pCO2 can enable the recovery of algal communities. By understanding the ecological processes responsible for driving shifts in community composition, we can better assess how communities are likely to be altered by ocean acidification.
    Keywords: Abundance; Alkalinity, total; Alkalinity, total, standard deviation; Aragonite saturation state; Aragonite saturation state, standard deviation; Benthos; Bicarbonate ion; Bicarbonate ion, standard deviation; Calcite saturation state; Calcite saturation state, standard deviation; Calculated using CO2SYS; Calculated using seacarb after Nisumaa et al. (2010); Carbon, inorganic, dissolved; Carbon, inorganic, dissolved, standard deviation; Carbonate ion; Carbonate ion, standard deviation; Carbonate system computation flag; Carbon dioxide; CO2 vent; Coast and continental shelf; Community composition and diversity; Complexity; Coverage; Entire community; EXP; Experiment; Experiment duration; Field experiment; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Gross community production of oxygen; Net community production, oxygen; North Pacific; OA-ICC; Ocean Acidification International Coordination Centre; Partial pressure of carbon dioxide, standard deviation; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); pH; pH, standard deviation; Primary production/Photosynthesis; Replicate; Respiration; Respiration rate, community; Rocky-shore community; Salinity; Salinity, standard deviation; Season; Shikine; Site; Temperate; Temperature, water; Type
    Type: Dataset
    Format: text/tab-separated-values, 2614 data points
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  • 8
    Publication Date: 2024-06-12
    Description: Surveys of seagrass associated fisheries were conducted as part of a large-scale seagrass ecosystem services assessment conducted across five countries: Malaysia, Indonesia, Thailand, Philippines and Timor-Leste under the International Climate Initiative (IKI): Seagrass Ecosystem Services Project (https://www.dugongseagrass.org/projects/seagrass-ecosystem-services-project/). To survey seagrass-associated biodiversity, data collectors used Baited Remote Underwater Video systems (BRUVS) and footage was analysed by an observer, trained in fish identification, for relative abundance (MaxN) and species richness between July 2022 – June 2023. A total of 325 hours were collected from seagrass meadows across the Indo-Pacific, with depth ranges of 0.5 – 8.4 metres. Data points were selected by local NGO's and/or community members, and placed a minimum of 50m apart.
    Keywords: Ablennes hians; Abudefduf sexfasciatus; Abudefduf vaigiensis; Acanthochromis polyacanthus; Acanthurus bahianus; Acanthurus nigricaudus; Acanthurus thompsoni; Acanthurus triostegus; Acentrogobius caninus; Acreichthys tomentosus; Aeoliscus strigatus; Alepes apercna; Alepes melanoptera; Aluterus scriptus; Amanses scopas; Ambassis gymnocephalus; Amblyglyphidodon curacao; Amblyglyphidodon ternatensis; Amblygobius buanensis; Amblygobius sphynx; Amphiprion clarkii; Amphiprion polymnus; Anampses caeruleopunctatus; Anampses melanurus; Aphareus rutilans; Apogon endekataenia; Apogon kallopterus; Apogon trimaculatus; Archamia bleekeri; Area/locality; Arius maculatus; Arothron hispidus; Arothron immaculatus; Arothron manilensis; Arothron reticularis; Arothron stellatus; Aspidontus taeniatus; Asterropteryx striata; Atherinomorus lacunosus; Atule mate; Aulostomus chinensis; Aulostomus strigosus; Balistapus undulatus; Bodianus bilunulatus; BRUV; Calotomus carolinus; Calotomus spinidens; Calotomus viridescens; Cantherhines dumerilii; Cantherhines pardalis; Cantheschenia grandisquamis; Canthigaster bennetti; Canthigaster coronata; Canthigaster valentini; Carangoides orthogrammus; Carangoides praeustus; Caranx ignobilis; Caranx melampygus; Caranx sexfasciatus; Centropyge bicolor; Centropyge flavipectoralis; Centropyge vrolikii; Cephalopholis cyanostigma; Chaetodon auriga; Chaetodon kleinii; Chaetodon lunulatus; Chaetodon melannotus; Chaetodon trifascialis; Chaetodon vagabundus; Cheilinus chlorourus; Cheilinus trilobatus; Cheilodipterus artus; Cheilodipterus macrodon; Cheilodipterus parazonatus; Cheilodipterus quinquelineatus; Chelio inermis; Chelonodon patoca; Choerodon anchorago; Choerodon jordani; Chromis notata; Chromis viridis; Chrysiptera cymatilis; Chrysiptera tricincta; Cirrhilabrus condei; Cirrhilabrus temmincki; Cloud cover; Colurodontis paxmani; Comment; Coris gaimard; Coris pictoides; Country; Crenimugil crenilabis; Cryptocentrus cinctus; Cryptocentrus sericus; Ctenochaetus flavicauda; Ctenochaetus striatus; Dascyllus aruanus; Dascyllus reticulatus; Dascyllus trimaculatus; Data source; DATE/TIME; DEPTH, water; Dexillichthys aspilos; Dexillus muelleri; Diagramma pictum; Diodon holocanthus; Diodon hystrix; Diproctacanthus xanthurus; Dischistodus chrysopoecilus; Dischistodus fasciatus; Dischistodus perspicillatus; Dischistodus prosopotaenia; Dischistodus pseudochrysopoecilus; Echeneis naucrates; Echidna nebulosa; Epinephelus amblycephalus; Epinephelus areolatus; Epinephelus bleekeri; Epinephelus merra; Epinephelus rivulatus; Epinephelus sexfasciatus; Epinephelus stictus; Eubalichthys caeruleoguttatus; Event label; Eviota bifasciata; Fishing intensity; Fistularia commersonii; Gerres argyreus; Gerres erythrourus; Gerres filamentosus; Gerres oyena; Gnathanodon speciosus; GPS, Garmin, GPSMAP 79s; Gunnelichthys curiosus; Gymnocaesio gymnopterus; Gymnocranius elongatus; Gymnocranius euanus; Gymnocranius grandoculis; Gymnosarda unicolor; Gymnothorax albimarginatus; Gymnothorax buroensis; Gymnothorax cribroris; Gymnothorax flavimarginatus; Gymnothorax tile; Gymnothorax undulatus; Halicampus grayi; Halichoeres argus; Halichoeres chloropterus; Halichoeres chrysotaenia; Halichoeres chrysus; Halichoeres marginatus; Halichoeres melanochir; Halichoeres melanurus; Halichoeres pallidus; Halichoeres papilionaceus; Halichoeres scapularis; Halichoeres schwartzii; Halichoeres trimaculatus; Hemigymnus melapterus; Hemiramphus brasiliensis; Heniochus acuminatus; Heniochus diphreutes; Hexanematichthys sagor; Hipposcarus longiceps; Hologymnosus annulatus; Hoplolatilus cuniculus; Hypoatherina barnesi; Hyporhamphus limbatus; ID_Ba_1; ID_Ba_10; ID_Ba_11; ID_Ba_12; ID_Ba_13; ID_Ba_14; ID_Ba_15; ID_Ba_16; ID_Ba_17; ID_Ba_18; ID_Ba_19; ID_Ba_2; ID_Ba_20; ID_Ba_21; ID_Ba_22; ID_Ba_3; ID_Ba_4; ID_Ba_5; ID_Ba_6; ID_Ba_7; ID_Ba_9; ID_Bu_1; ID_Bu_10; ID_Bu_11; ID_Bu_12; ID_Bu_13; ID_Bu_14; ID_Bu_15; ID_Bu_16; ID_Bu_17; ID_Bu_18; ID_Bu_19; ID_Bu_2; ID_Bu_20; ID_Bu_21; ID_Bu_22; ID_Bu_23; ID_Bu_24; ID_Bu_3; ID_Bu_4; ID_Bu_5; ID_Bu_6; ID_Bu_7; ID_Bu_8; ID_Bu_9; ID_Ta_1; ID_Ta_11; ID_Ta_12; ID_Ta_13; ID_Ta_14; ID_Ta_15; ID_Ta_16; ID_Ta_17; ID_Ta_18; ID_Ta_19; ID_Ta_20; ID_Ta_21; ID_Ta_22; ID_Ta_23; ID_Ta_24; ID_Ta_4; ID_Ta_5; ID_Ta_6; ID_Ta_7; ID_Ta_8; ID_Ta_9; Identification; Indonesia; Indo-Pacific; Istiblennius lineatus; Kaupichthys brachychirus; Labroides bicolor; Labroides dimidiatus; Lagocephalus spadiceus; Lagocephalus suezensis; LATITUDE; Leptojulis cyanopleura; Leptoscarus vaigiensis; Lethrinus atkinsoni; Lethrinus erythropterus; Lethrinus genivittatus; Lethrinus harak; Lethrinus lentjan; Lethrinus microdon; Lethrinus obsoletus; Lethrinus olivacelus; Lethrinus ornatus; lethrinus ravus; Lethrinus rubrioperculatus; Lethrinus semicinctus; Lethrinus variegatus; Liza vaigiensis; LONGITUDE; Lutjanus bohar; Lutjanus carponotatus; Lutjanus ehrenbergii; Lutjanus fulviflamma; Lutjanus fulvus; Lutjanus gibbus; Lutjanus lemniscatus; Lutjanus maxweberi; Lutjanus russelli; Lutjanus vitta; Macropharyngodon negrosensis; Macrorhamphosodes platycheilus; Malacanthus brevirostris; Malaysia; Megalaspis cordyla; Megalops cyprinoides; Meiacanthus abruptus; Meiacanthus grammistes; Monacanthus chinensis; Monodactylus argenteus; Monotaxis heterodon; Mulloidichthys flavolineatus; Mulloidichthys vanicolensis; MULT; Multiple investigations; MY_Set_1; MY_Set_10; MY_Set_11; MY_Set_12; MY_Set_13; MY_Set_14; MY_Set_15; MY_Set_16; MY_Set_17; MY_Set_18; MY_Set_19; MY_Set_2; MY_Set_20; MY_Set_21; MY_Set_3; MY_Set_4; MY_Set_5; MY_Set_6; MY_Set_7; MY_Set_8; MY_Set_9; MY_Sibu_1; MY_Sibu_10; MY_Sibu_11; MY_Sibu_12; MY_Sibu_2; MY_Sibu_3; MY_Sibu_4; MY_Sibu_5; MY_Sibu_6; MY_Sibu_7; MY_Sibu_8; MY_Sibu_9; MY_Ting_1; MY_Ting_10; MY_Ting_11; MY_Ting_12; MY_Ting_13; MY_Ting_14; MY_Ting_15; MY_Ting_16; MY_Ting_17; MY_Ting_18; MY_Ting_19; MY_Ting_2; MY_Ting_20; MY_Ting_21; MY_Ting_22; MY_Ting_23; MY_Ting_24; MY_Ting_3; MY_Ting_4; MY_Ting_5; MY_Ting_6; MY_Ting_7; MY_Ting_8; MY_Ting_9; Myrichthys colubrinus; Myrichthys maculosus; Naso thynnoides; Naso unicornis; Nemipterus furcosus; Nemipterus nematophorus; Neoglyphidodon melas; Neomyxus leuciscus; Novaculichthys macrolepidotus; Novaculichthys taeniourus; Novaculoides macrolepidotus; Ostorhinchus angustatus; Ostorhinchus cavitensis; Ostorhinchus fasciatus; Ostorhinchus margaritophorus; Ostorhinchus nigrofasciatus; Ostorhinchus taeniophorus; Oxycheilinus bimaculatus; Parachaetodon ocellatus; Paramonacanthus curtorhynchos; Paramonacanthus japonicus; Paramonacanthus tricuspis; Parapercis cylindrica; Parapercis diplospilus; Parapercis lineopunctata; Parapercis snyderi; Parapercis tetracantha; Parapercis xanthozona; Parastromateus niger; Parupeneus barberinoides; Parupeneus barberinus; Parupeneus crassilabris; Parupeneus cyclostomus; Parupeneus indicus; Parupeneus macronema; Parupeneus macronemus; Parupeneus multifasciatus; Pastinachus sephen; Pelates quadrilineatus; Pentapodus bifasciatus; Pentapodus paradiseus; Pentapodus setosus; Pentapodus trivittatus; Pervagor janthinosoma; Pervagor nigrolineatus; Petroscirtes breviceps; Petroscirtes mitratus; Petroscirtes variabilis; PH_Che_1; PH_Che_2; PH_Che_3; PH_Che_4; PH_Che_5; PH_Che_6; PH_Dia_1; PH_Dia_2; PH_Dia_3; PH_Dia_4; PH_Dia_5; PH_GIE_1; PH_GIE_2; PH_GIE_3; PH_GIE_4; PH_GIE_5; PH_GIW_1; PH_GIW_2; PH_GIW_3; PH_GIW_4; PH_GIW_5; PH_GIW_6; PH_JI_1; PH_JI_10; PH_JI_11; PH_JI_12; PH_JI_13; PH_JI_14; PH_JI_15; PH_JI_16; PH_JI_17; PH_JI_18; PH_JI_19; PH_JI_2; PH_JI_20; PH_JI_21; PH_JI_22; PH_JI_23; PH_JI_3; PH_JI_4; PH_JI_5; PH_JI_6; PH_JI_7; PH_JI_8; PH_JI_9; PH_Ocam_1; PH_Ocam_10; PH_Ocam_2; PH_Ocam_3; PH_Ocam_4; PH_Ocam_5; PH_Ocam_6; PH_Ocam_7; PH_Ocam_8; PH_Ocam_9; Philippines; Platax teira; Platybelone argalus; Plectroglyphidodon leucozonus; Plot of land; Plotosus lineatus; Pomacanthus xanthometopon; Pomacentrus amboinensis; Pomacentrus imitator; Pomacentrus melanochir; Pomacentrus nagasakiensis; Pomacentrus simsiang; Pomacentrus smithi;
    Type: Dataset
    Format: text/tab-separated-values, 112197 data points
    Location Call Number Expected Availability
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  • 9
    Publication Date: 2024-06-12
    Description: Surveys of seagrass morphometrics were conducted as part of a large-scale seagrass ecosystem services assessment conducted across five countries: Malaysia, Indonesia, Thailand, Philippines and Timor-Leste under the International Climate Initiative (IKI): Seagrass Ecosystem Services Project (https://www.dugongseagrass.org/projects/seagrass-ecosystem-services-project/), between July 2022 and April 2023. Data points were selected by local NGO's and/or community members. Five random 0.25 m² quadrats were placed around each Baited Remote Underwater Video system (BRUV) point, where data on seagrass cover, seagrass species composition, algae cover, canopy height, epiphyte cover and sediment type were recorded (modified from Jones et al., 2021). Data were collected from a total of 880 quadrats, observing nine seagrass species across Indo-Pacific sample sites.
    Keywords: According to McKenzie et al. (2003); Algae, cover; Area/locality; BRUV; Canopy height; Country; Cymodocea rotundata, cover; DATE/TIME; Enhalus acoroides, cover; Epiphytes, cover; Event label; GPS, Garmin, GPSMAP 79s; Halodule pinifolia, cover; Halodule uninervis, cover; Halophila ovalis, cover; ID_Ba_1; ID_Ba_10; ID_Ba_2; ID_Ba_3; ID_Ba_4; ID_Ba_5; ID_Ba_6; ID_Ba_7; ID_Ba_8; ID_Ba_9; ID_Bu_1; ID_Bu_10; ID_Bu_11; ID_Bu_12; ID_Bu_2; ID_Bu_3; ID_Bu_4; ID_Bu_5; ID_Bu_6; ID_Bu_7; ID_Bu_8; ID_Bu_9; ID_Ta_1; ID_Ta_10; ID_Ta_11; ID_Ta_12; ID_Ta_2; ID_Ta_3; ID_Ta_4; ID_Ta_5; ID_Ta_6; ID_Ta_7; ID_Ta_8; ID_Ta_9; Identification; Indonesia; Indo-Pacific; LATITUDE; LONGITUDE; Malaysia; MULT; Multiple investigations; MY_Set_1; MY_Set_2; MY_Set_3; MY_Set_4; MY_Set_5; MY_Set_6; Oceana serrulata, cover; PH_Ba_1; PH_Ba_2; PH_Bv_1; PH_Bv_2; PH_Che_4; PH_Che_5; PH_Che_6; PH_Dia_3; PH_Dia_4; PH_Dia_5; PH_GIE_1; PH_GIE_2; PH_GIE_3; PH_GIE_4; PH_GIE_5; PH_GIW_1; PH_GIW_2; PH_GIW_3; PH_GIW_4; PH_GIW_5; PH_GIW_6; PH_JI_1; PH_JI_10; PH_JI_11; PH_JI_12; PH_JI_13; PH_JI_14; PH_JI_15; PH_JI_16; PH_JI_17; PH_JI_18; PH_JI_19; PH_JI_2; PH_JI_20; PH_JI_21; PH_JI_22; PH_JI_23; PH_JI_3; PH_JI_4; PH_JI_5; PH_JI_6; PH_JI_7; PH_JI_8; PH_JI_9; PH_Mac_1; PH_Mac_2; PH_Mac_3; PH_Mad_1; PH_Mad_2; PH_Mad_3; PH_Mad_4; PH_Mad_5; PH_Mad_6; PH_Mang_1; PH_Mang_2; PH_Mang_3; PH_Ocam_1; PH_Ocam_10; PH_Ocam_2; PH_Ocam_3; PH_Ocam_4; PH_Ocam_5; PH_Ocam_6; PH_Ocam_7; PH_Ocam_8; PH_Ocam_9; PH_Tag_1; PH_Tag_2; PH_Tag_3; Philippines; Quadrat number; Seagrass; Seagrass, cover; seagrass ecosystem services; seagrass traits; Season; Sediment type; Site; small-scale fishery; Species richness level; Syringodium isoetifolium, cover; TH_Mook_1; TH_Mook_10; TH_Mook_11; TH_Mook_12; TH_Mook_13; TH_Mook_14; TH_Mook_15; TH_Mook_16; TH_Mook_17; TH_Mook_18; TH_Mook_19; TH_Mook_2; TH_Mook_20; TH_Mook_21; TH_Mook_22; TH_Mook_23; TH_Mook_24; TH_Mook_25; TH_Mook_26; TH_Mook_27; TH_Mook_28; TH_Mook_29; TH_Mook_3; TH_Mook_30; TH_Mook_31; TH_Mook_32; TH_Mook_33; TH_Mook_34; TH_Mook_35; TH_Mook_36; TH_Mook_37; TH_Mook_38; TH_Mook_39; TH_Mook_4; TH_Mook_40; TH_Mook_41; TH_Mook_42; TH_Mook_43; TH_Mook_44; TH_Mook_45; TH_Mook_46; TH_Mook_47; TH_Mook_48; TH_Mook_49; TH_Mook_5; TH_Mook_50; TH_Mook_6; TH_Mook_7; TH_Mook_8; TH_Mook_9; TH_Suk_1; Thailand; Thalassia hemprichii, cover; Thalassodendron ciliatum, cover; Timor-Leste; TL_Bel_1; TL_Bel_2; TL_Bel_3; TL_Bel_4; TL_Bel_5; TL_Bel_6; TL_Bel_7; TL_Bel_8; TL_Biq_1; TL_Biq_2; TL_Biq_3; TL_Biq_4; TL_Biq_5; TL_Biq_6; TL_Biq_7; TL_Biq_8
    Type: Dataset
    Format: text/tab-separated-values, 21120 data points
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  • 10
    Publication Date: 2023-12-20
    Description: This book constitutes the refereed proceedings of the 13th IFIP WG 2.13 International Conference on Open Source Systems, OSS 2017, held in Buenos Aires, Argentina, in May 2017. The 16 revised full papers and 3 short papers presented were carefully reviewed and selected from 32 submissions. The papers cover a wide range of topics related to free, libre, and open source software (FLOSS), including: licensing, strategies, and practices; case studies; projects, communication, and participation; tools; and project management, development and evaluation.
    Keywords: QA75.5-76.95 ; open access ; Linux ; open source software ; collaboration ; information systems ; bic Book Industry Communication::U Computing & information technology::UY Computer science
    Language: English
    Format: image/jpeg
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